Device recall
Z-0897-2011: Precedence SPECT/CT System, Precedence 16 3/8, Upper Patient Pallet, A single…
FDA device recall · Class II · Phillips Nuclear Medicine
Key facts
| Recall number (Z-number) | Z-0897-2011 |
|---|---|
| Recall event | 51274 |
| Product | Precedence SPECT/CT System, Precedence 16 3/8, Upper Patient Pallet, A single photon nuclear medicine and image from an X-ray computed tomography system, Model Number: 4535 602 50851, Catalog Number: 882350, Product is manufactured by Philips Medical Systems (Cleveland), Inc. Cleveland, OH Intended… |
| Product code | INQ |
| Recalling firm | Phillips Nuclear Medicine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2011 |
| 510(k) numbers | K051351 |
| FEI number | 1525965 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database